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ANVISA registration 81487669005Active

PERIPHERAL ANGIOPLASTY BALLOON CATHETER

ANVISA Registration Number: 81487669005GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDAZYLOX-TONBRIDGE MEDICAL TECHNOLOGY CO., LTD.Risk Class II
Verified
Device names
Technical name
PERIPHERAL ANGIOPLASTY BALLOON CATHETER
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PT: CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Commercial name
Cateter balão ZENFlow II HP PTA
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Risk class
Class II
Registration details
Registration Number
81487669005
Process Number
25351289287202433
CNPJ
20503395000152
Company information
Registration Holder
GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDA
Manufacturer
ZYLOX-TONBRIDGE MEDICAL TECHNOLOGY CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
May 28, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for PERIPHERAL ANGIOPLASTY BALLOON CATHETER in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 81487669005 and manufactured by ZYLOX-TONBRIDGE MEDICAL TECHNOLOGY CO., LTD.. The registration is held by GF MEDIKA IMPORTAÇÃO E EXPORTAÇÃO LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.